Le Son C, Liang Pengfei, Lowry Augustus J, Yang Huanghe
Department of Biochemistry, Duke University Medical Center, Durham, NC, United States.
Department of Neurobiology, Duke University Medical Center, Durham, NC, United States.
Front Physiol. 2021 Nov 19;12:787773. doi: 10.3389/fphys.2021.787773. eCollection 2021.
The transmembrane protein 16 (TMEM16) family consists of Ca-activated ion channels and Ca-activated phospholipid scramblases (CaPLSases) that passively flip-flop phospholipids between the two leaflets of the membrane bilayer. Owing to their diverse functions, TMEM16 proteins have been implicated in various human diseases, including asthma, cancer, bleeding disorders, muscular dystrophy, arthritis, epilepsy, dystonia, ataxia, and viral infection. To understand TMEM16 proteins in health and disease, it is critical to decipher their molecular mechanisms of activation gating and regulation. Structural, biophysical, and computational characterizations over the past decade have greatly advanced the molecular understanding of TMEM16 proteins. In this review, we summarize major structural features of the TMEM16 proteins with a focus on regulatory mechanisms and gating.
跨膜蛋白16(TMEM16)家族由钙激活离子通道和钙激活磷脂翻转酶(CaPLSases)组成,后者可使磷脂在膜双层的两个小叶之间被动翻转。由于其功能多样,TMEM16蛋白与多种人类疾病有关,包括哮喘、癌症、出血性疾病、肌肉萎缩症、关节炎、癫痫、肌张力障碍、共济失调和病毒感染。为了了解健康和疾病状态下的TMEM16蛋白,关键是要破译其激活门控和调节的分子机制。过去十年的结构、生物物理和计算表征极大地推进了对TMEM16蛋白的分子理解。在本综述中,我们总结了TMEM16蛋白的主要结构特征,重点关注调节机制和门控。